Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
International Society for Gastrointestinal Hereditary Tumours |
RCV000076271 | SCV000107296 | likely benign | Lynch syndrome | 2013-09-05 | reviewed by expert panel | research | Intronic substitution with no effect on splicing, tested with NMD inhibitor |
Gene |
RCV001723647 | SCV001950814 | benign | not provided | 2019-03-10 | criteria provided, single submitter | clinical testing |